Multi-omics analysis using antibody-based in situ biotinylation technique suggests the mechanism of Cajal body formation

Membrane-less subcellular compartments play important roles in various cellular functions. Although techniques exist to identify components of cellular bodies, a comprehensive method for analyzing both static and dynamic states has not been established. Here, we apply an antibody-based in situ biotinylation proximity-labeling technique to identify components of static and dynamic nuclear bodies. Using this approach, we comprehensively identify DNA, RNA, and protein components of Cajal bodies (CBs) and then clarify their interactome. By inhibiting transcription, we capture dynamic changes in CBs. Our analysis reveals that nascent small nuclear RNAs (snRNAs) transcribed in CBs contribute to CB formation by assembling RNA-binding proteins, including frontotemporal dementia-related proteins, RNA-binding motif proteins, and heterogeneous nuclear ribonucleoproteins.

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Publication Details

Journal
Cell Reports
Published
2024-09-01
DOI
https://doi.org/10.1016/j.celrep.2024.114734
Citations
6
Primary Topic
Biotin and Related Studies
Type
article
Field-Weighted Citation Impact
1.96

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article

Multi-omics analysis using antibody-based in situ biotinylation technique suggests the mechanism of Cajal body formation

Yuki Yamaguchi, Nobuyoshi Akimitsu, Akihide Ryo, Atsushi Toyoda et al.
6 citations
Cell Reports
Biotin and Related Studies
1.96
article

Multi-omics analysis using antibody-based in situ biotinylation technique suggests the mechanism of Cajal body formation

Yuki Yamaguchi, Nobuyoshi Akimitsu, Akihide Ryo, Atsushi Toyoda, Hidehisa Takahashi, Yoko Ike, Ryota Abe, Yayoi Kimura, Rena Onoguchi‐Mizutani, Yoko Ino, Keiko Horiuchi, Keisuke Noguchi, Hiroshi Doi, Fumiaki Tanaka, Hidefumi Suzuki, Tomohiko Akiyama, Yutaka Suzuki, Shintaro Ogawa
article en
6 citations

Abstract

Membrane-less subcellular compartments play important roles in various cellular functions. Although techniques exist to identify components of cellular bodies, a comprehensive method for analyzing both static and dynamic states has not been established. Here, we apply an antibody-based in situ biotinylation proximity-labeling technique to identify components of static and dynamic nuclear bodies. Using this approach, we comprehensively identify DNA, RNA, and protein components of Cajal bodies (CBs) and then clarify their interactome. By inhibiting transcription, we capture dynamic changes in CBs. Our analysis reveals that nascent small nuclear RNAs (snRNAs) transcribed in CBs contribute to CB formation by assembling RNA-binding proteins, including frontotemporal dementia-related proteins, RNA-binding motif proteins, and heterogeneous nuclear ribonucleoproteins.

Cell ReportsVol. 43(9)
National Institute of Genetics (JP), Tokyo Institute of Technology (JP), Yokohama City University Medical Center (JP), National Institute of Infectious Diseases (JP), The University of Tokyo (JP), Yokohama City University (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 15%
Biotin and Related Studies
1.96
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